Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 5:143281964 (forward strand) | View in location tab

Co-located

with COSMIC COSM1672002 (T/A)

Most severe consequence
Clinical significance

Synonyms

LSDB 2186

This variation has 16 HGVS names - click the plus to show

5:g.143281964T>A
ENST00000394464.4:c.2259A>T
ENSP00000377977.2:p.Leu753Phe
ENST00000231509.5:c.2262A>T
ENSP00000231509.3:p.Leu754Phe
ENST00000504572.3:c.2262A>T
ENSP00000422518.1:p.Leu754Phe
ENST00000503201.1:c.2259A>T
ENSP00000427672.1:p.Leu753Phe
ENST00000424646.4:c.2181A>T
ENSP00000405282.2:p.Leu727Phe
ENST00000343796.4:c.2259A>T
ENSP00000343205.2:p.Leu753Phe
ENST00000415690.4:c.2181+604A>T
ENST00000394466.4:c.2262A>T
ENSP00000377979.2:p.Leu754Phe

Variation displays